Author(s): Pignatelli, D ; Carvalho, B ; Palmeiro, A ; Barros, A ; Guerreiro, SG ; Macut, D
Date: 2020
Persistent ID: https://hdl.handle.net/10216/145290
Origin: Repositório Aberto da Universidade do Porto
Subject(s): 21OH deficiency; adrenal cortex; androgen excess syndromes; CAH—congenital adrenal hyperplasia; disorders of sex development; endocrine genetics; genotyping; rare diseases
